A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191005



Internal ID21329864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149764542..149764542hg38UCSC Ensembl
chr3:149482329..149482329hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949313
Supporting Variants
SamplesHG002
Known GenesANKUB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191005
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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